Lithium hydroxide, monohydrate → HCID 59127134、化合物

HRID 1011666ノート

反応式

HRID 1011666 の反応式
O.[OH-].[Li+].CC([Si](C)(C)[O:9][C:10]1[CH:11]=[C:12]([CH:21]=[C:22]([O:24][C@@H:25]([CH3:35])[CH2:26][O:27][Si:28]([C:31]([CH3:34])([CH3:33])[CH3:32])([CH3:30])[CH3:29])[CH:23]=1)[C:13]([NH:15][C:16]1[S:17][CH:18]=[CH:19][N:20]=1)=[O:14])(C)C>C1COCC1>[CH3:32][C:31]([Si:28]([CH3:30])([CH3:29])[O:27][CH2:26][C@@H:25]([O:24][C:22]1[CH:21]=[C:12]([CH:11]=[C:10]([OH:9])[CH:23]=1)[C:13]([NH:15][C:16]1[S:17][CH:18]=[CH:19][N:20]=1)=[O:14])[CH3:35])([CH3:33])[CH3:34]

参加物

4

反応物 2

HCID 168937Lithium hydroxide, monohydrateHCID 536296183-{[(1,1-dimethylethyl)(dimethyl)silyl]oxy}-5-[((1S)-2-{[(1,1-dimethylethyl)(dimethyl)silyl]oxy}-1-methylethyl)oxy]-N-1,3-thiazol-2-ylbenzamide

生成物 1

HCID 59127134HCID 59127134、化合物収率 73%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

An aqueous solution of lithium hydroxide monohydrate (0.304 g, 7.25 mmol) was added to a solution of 3-{[(1,1-dimethylethyl)(dimethyl)silyl]oxy}-5-[((1S)-2-{[(1,1-dimethylethyl)(dimethyl)silyl]oxy}-1-methylethyl)oxy]-N-1,3-thiazol-2-ylbenzamide (1.552 g, 2.90 mmol) in THF (40 mL) and stirred at RT overnight. The THF was removed in vacuo and the residual solution adjusted to pH 7 by addition of 1N hydrochloric acid (7.25 mL). A gum formed, and the solution was filtered and the gum dissolved in methanol. The filtrate was partitioned with ethyl acetate (75 mL) and the organics washed with brine, dried (MgSO4), combined with the methanol solution and evaporated to a residue which was chromatographed on silica, eluting with 40% ethyl acetate in isohexane, to give the required product (0.865 g)

後処理

  1. customThe THF was removed in vacuo
  2. additionthe residual solution adjusted to pH 7 by addition of 1N hydrochloric acid (7.25 mL)
  3. customA gum formed
  4. filtrationthe solution was filtered
  5. dissolutionthe gum dissolved in methanol
  6. customThe filtrate was partitioned with ethyl acetate (75 mL)
  7. washthe organics washed with brine
  8. dry with materialdried (MgSO4)
  9. customevaporated to a residue which
  10. customwas chromatographed on silica
  11. washeluting with 40% ethyl acetate in isohexane

出典と根拠

ORDレコード
ord-b76897a7e70a45a0b2fba909fac6df83
出典データセット
uspto-grants-2011_07
特許番号
US07977328B2

反応ノート

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